CL2009000815A1 - Compounds derived from phenylhydroxymethylpyrrolidine, beta 3 adrenergic receptor agonist; pharmaceutical composition comprising them; use in the treatment of overactive bladder, urge urinary incontinence and urinary urgency. - Google Patents
Compounds derived from phenylhydroxymethylpyrrolidine, beta 3 adrenergic receptor agonist; pharmaceutical composition comprising them; use in the treatment of overactive bladder, urge urinary incontinence and urinary urgency.Info
- Publication number
- CL2009000815A1 CL2009000815A1 CL2009000815A CL2009000815A CL2009000815A1 CL 2009000815 A1 CL2009000815 A1 CL 2009000815A1 CL 2009000815 A CL2009000815 A CL 2009000815A CL 2009000815 A CL2009000815 A CL 2009000815A CL 2009000815 A1 CL2009000815 A1 CL 2009000815A1
- Authority
- CL
- Chile
- Prior art keywords
- treatment
- phenylhydroxymethylpyrrolidine
- beta
- pharmaceutical composition
- receptor agonist
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/428—Thiazoles condensed with carbocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/06—Anti-spasmodics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/10—Drugs for disorders of the urinary system of the bladder
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/12—Antidiuretics, e.g. drugs for diabetes insipidus
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Urology & Nephrology (AREA)
- Diabetes (AREA)
- Epidemiology (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyrrole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pyridine Compounds (AREA)
Abstract
COMPUESTO DERIVADO DE FENILHIDROXIMETILPIRROLIDINA DE FÓRMULA IA, O UNA DE SUS SALES FARMACÉUTICAMENTE ACEPTABLES, O UN ESTEREOISÓMERO DEL MISMO, O UNA SAL FARMACÉUTICAMENTE ACEPTABLE DEL ESTEREOISÓMERO DEL MISMO DONDE R3 Y N SON COMO SE DEFINEN EN LA MEMORIA DESCRIPTIVA COMPOSICIÓN FARMACÉUTICA QUE COMPRENDE DICHO COMPUESTO Y UN VEHICULO FARMACÉUTICAMENTE ACEPTABLE; Y USO DE UNA CANTIDAD TERAPÉUTICAMENTE EFICAZ DE DICHO COMPUESTO QUE SIRVE PARA PREPARAR UN MEDICAMENTO ÚTIL PARA EL TRATAMIENTO O PREVENCIÓN DE UNA ENFERMEDAD O TRASTORNO MEDIADO POR LA ACTIVACIÓN DEL ADRENOCEPTOR ß3 .COMPOUND DERIVED FROM PHENYLHYDROXIMETHYLPYRROLIDINE OF FORMULA IA, OR ONE OF ITS PHARMACEUTICALLY ACCEPTABLE SALTS, OR A STEREOISOMER OF THE SAME, OR A PHARMACEUTICALLY ACCEPTABLE SALT OF THE STEREOISOMER AND DESCRIPTION OF THE SAME PHARMACEUTICAL MEMORY AND DESCRIPTION OF THE SAME DONOMOUS RICHNEY COMPOUND IN THE SAME PHARMACEUTICAL MEMORY AND DESCRIPTION IN THE SAME DONOMINARY COMPOUND3. PHARMACEUTICALLY ACCEPTABLE VEHICLE; AND USE OF A THERAPEUTICALLY EFFECTIVE AMOUNT OF SAID COMPOUND THAT IS USED TO PREPARE A USEFUL MEDICINE FOR THE TREATMENT OR PREVENTION OF A DISEASE OR DISORDER MEDIATED BY THE ACTIVATION OF THE ß3 ADRENOCEPTOR.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12306308P | 2008-04-04 | 2008-04-04 | |
| US20604309P | 2009-01-27 | 2009-01-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2009000815A1 true CL2009000815A1 (en) | 2009-08-21 |
Family
ID=40671093
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL2009000815A CL2009000815A1 (en) | 2008-04-04 | 2009-04-03 | Compounds derived from phenylhydroxymethylpyrrolidine, beta 3 adrenergic receptor agonist; pharmaceutical composition comprising them; use in the treatment of overactive bladder, urge urinary incontinence and urinary urgency. |
Country Status (42)
Families Citing this family (61)
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| PE20091825A1 (en) * | 2008-04-04 | 2009-12-04 | Merck & Co Inc | HYDROXIMETHYL PYRROLIDINES AS AGONISTS OF THE BETA 3 ADRENERGIC RECEPTOR |
| BR112012004333A2 (en) * | 2009-08-27 | 2015-09-08 | Merck Sharp & Dohme | compound, pharmaceutical composition, and method for treating or preventing a disease or disorder. |
| AU2010303811B2 (en) * | 2009-10-07 | 2013-01-24 | Merck Sharp & Dohme Corp. | Combination therapy using a beta 3 adrenergic receptor agonist and an antimuscarinic agent |
| WO2011137054A1 (en) | 2010-04-30 | 2011-11-03 | Merck Sharp & Dohme Corp. | Novel beta 3 adrenergic receptor agonists |
| CA2805427A1 (en) * | 2010-07-23 | 2012-01-26 | Merck Sharp & Dohme Corp. | Novel pyrrolidine derived beta 3 adrenergic receptor agonists |
| SG10201506076TA (en) * | 2010-08-03 | 2015-09-29 | Altherx Inc | Combinations of beta - 3 adrenergic receptor agonists and muscarinic receptor antagonists for treating overactive bladder |
| US9907767B2 (en) | 2010-08-03 | 2018-03-06 | Velicept Therapeutics, Inc. | Pharmaceutical compositions and the treatment of overactive bladder |
| US9522129B2 (en) | 2010-08-03 | 2016-12-20 | Velicept Therapeutics, Inc. | Pharmaceutical Combination |
| GB2484713A (en) | 2010-10-21 | 2012-04-25 | Optovate Ltd | Illumination apparatus |
| EP2742030B1 (en) * | 2011-08-11 | 2016-07-27 | Bayer Intellectual Property GmbH | 1,2,4-triazolyl-substituted ketoenols for use in plant protection |
| US9809536B2 (en) | 2011-10-27 | 2017-11-07 | Merck Sharp & Dohme Corp. | Process for making beta 3 agonists and intermediates |
| WO2013062881A1 (en) * | 2011-10-27 | 2013-05-02 | Merck Sharp & Dohme Corp. | Process for making beta 3 agonists and intermediates |
| CN104053771B (en) | 2011-11-18 | 2016-11-09 | 科德克希思公司 | Biocatalysts for the preparation of hydroxy-substituted carbamates |
| SG11201404776PA (en) * | 2012-02-09 | 2014-09-26 | Altherx Inc | Combination of muscarinic receptor antagonists and beta- 3 adrenoceptor agonists for treating overactive bladder |
| JP2015178458A (en) * | 2012-07-25 | 2015-10-08 | 杏林製薬株式会社 | Benzene ring condensed nitrogen-containing 5-membered heterocyclic compound, or pharmacologically acceptable salt thereof |
| US9784726B2 (en) | 2013-01-08 | 2017-10-10 | Atrogi Ab | Screening method, a kit, a method of treatment and a compound for use in a method of treatment |
| AU2014243818B2 (en) | 2013-03-13 | 2017-04-20 | Flatley Discovery Lab, Llc | Pyridazinone compounds and methods for the treatment of cystic fibrosis |
| HUE045260T2 (en) * | 2013-03-15 | 2019-12-30 | Merck Sharp & Dohme | A process for the production of beta 3 antagonists and their intermediates |
| CN103232352B (en) * | 2013-05-11 | 2015-12-23 | 苏州永健生物医药有限公司 | (R)-4-(2-(2-hydroxyl-2-phenylethylamine base) ethyl) anilino carboxylate |
| CN103760286A (en) * | 2014-01-14 | 2014-04-30 | 北京万全德众医药生物技术有限公司 | Method for measuring optical purity of solifenacin succinate intermediate by high-performance liquid chromatography |
| KR102396753B1 (en) | 2014-06-11 | 2022-05-12 | 베나토알엑스 파마슈티컬스, 인크. | Beta-lactamase inhibitors |
| KR20170086659A (en) | 2014-12-03 | 2017-07-26 | 벨리셉트 테라퓨틱스, 인크. | Compositions and methods of using modified release solabegron for lower urinary tract symptoms |
| CA2973202A1 (en) * | 2015-01-20 | 2016-07-28 | Merck Sharp & Dohme Corp. | Factor xia inhibitors |
| PT3365321T (en) | 2015-10-23 | 2024-01-12 | B3Ar Therapeutics Inc | Solabegron zwitterion and uses thereof |
| WO2017210700A1 (en) * | 2016-06-03 | 2017-12-07 | Velicept Therapeutics, Inc. | Compositions and methods of using modified release solabegron for lower urinary tract symptoms |
| GB201705364D0 (en) | 2017-04-03 | 2017-05-17 | Optovate Ltd | Illumination apparatus |
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| AU2018282105A1 (en) | 2017-06-06 | 2019-12-12 | Urovant Sciences Gmbh | Dosing of vibegron for treatment of overactive bladder |
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| GB201718307D0 (en) | 2017-11-05 | 2017-12-20 | Optovate Ltd | Display apparatus |
| CN118078835A (en) * | 2017-12-21 | 2024-05-28 | 杏林制药株式会社 | Therapeutic agent for nocturnal frequency |
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| JP2022510084A (en) | 2018-12-05 | 2022-01-26 | ウロバント サイエンシズ ゲーエムベーハー | Use of Viveglon to treat overactive bladder symptoms in men with benign prostatic hyperplasia |
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| KR20220077914A (en) | 2019-10-03 | 2022-06-09 | 리얼디 스파크, 엘엘씨 | Illumination device comprising passive optical nanostructures |
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| CN114920771A (en) * | 2022-05-13 | 2022-08-19 | 苏州虞美景盛新药开发有限公司 | Novel synthesis process of intermediate of novel oral medicine for overactive bladder |
| US12048712B2 (en) | 2022-10-18 | 2024-07-30 | Bonafide Health, Llc | Beta-adrenergic agonist and muscarinic antagonist compositions and methods of using |
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| US6525202B2 (en) | 2000-07-17 | 2003-02-25 | Wyeth | Cyclic amine phenyl beta-3 adrenergic receptor agonists |
| DOP2003000587A (en) * | 2002-02-27 | 2003-08-30 | Pfizer Prod Inc | Ss3-ADRENERGIC RECEIVER AGONISTS |
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| FR2874011B1 (en) * | 2004-08-03 | 2007-06-15 | Sanofi Synthelabo | SULFONAMIDE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION |
| PE20091825A1 (en) * | 2008-04-04 | 2009-12-04 | Merck & Co Inc | HYDROXIMETHYL PYRROLIDINES AS AGONISTS OF THE BETA 3 ADRENERGIC RECEPTOR |
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2009
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- 2009-04-02 ES ES09726601T patent/ES2376278T3/en active Active
- 2009-04-02 PT PT09726601T patent/PT2276756E/en unknown
- 2009-04-02 KR KR1020127026256A patent/KR20120118086A/en not_active Withdrawn
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- 2009-04-02 US US12/417,239 patent/US8247415B2/en active Active
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- 2009-04-02 KR KR1020127015876A patent/KR101288798B1/en not_active Expired - Fee Related
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- 2012-06-20 US US13/527,934 patent/US8653260B2/en active Active
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